64 research outputs found
Iannone, Carol: National Council on the Humanities Nomination (1991): Correspondence 08
- Author
- Publication venue
- DigitalCommons@URI
- Publication date
- 06/04/1991
- Field of study
Severe paraneoplastic hypoglycemia in a patient with a gastrointestinal stromal tumor with an exon 9 mutation: a case report
- Author
- B Nilsson
- B Rikhof
- CD Fletcher
- D LeRoith
- D Pink
- Drew C Heiple
- EM Connolly
- F Mattioli
- FJ Service
- Glen J Weiss
- Guillermo A Escobar
- I Hostein
- J Lasota
- JD Teale
- K Hartmann
- K Hoekman
- K Hussain
- Linda Buckley
- M Carballo
- M Debiec-Rychter
- M Miettinen
- Martin D McCarter
- MC Heinrich
- ML Lux
- MM Beckers
- N Bourcigaux
- N Hizuka
- P Hamberg
- R Roskoski Jr.
- Rene Gonzalez
- RM Mehta
- T Tran
- Trevor L Nydam
- V Marks
- WG Goettsch
- WH Daughaday
- WH Daughaday
- William A Robinson
- Publication venue
- BioMed Central
- Publication date
- 01/01/2007
- Field of study
BACKGROUND: Non-islet cell tumor induced hypoglycemia (NICTH) is a very rare phenomenon, but even more so in gastrointestinal stromal tumors. It tends to present in large or metastatic tumors, and can appear at any time in the progression of the disease. We present herein a case of NICTH in a GIST tumor and report an exon 9 mutation associated to it. CASE PRESENTATION: A thirty nine year-old man with a recurrent, metastatic gastrointestinal stromal tumor presented to the hospital with nausea, dizziness, loss of consciousness, and profound hypoglycemia (20 mg/dL). There was no evidence of factitious hypoglycemia. He was stabilized with a continuous glucose infusion and following selective vascular embolization, the patient underwent debulking of a multicentric 40 cm × 25 cm × 10 cm gastrointestinal stromal tumor. After resection, the patient became euglycemic and returned to his normal activities. Tumor analysis confirmed excessive production of insulin-like growth factor II m-RNA and the precursor protein, "big" insulin-like growth factor II. Mutational analysis also identified a rare, 6 bp tandem repeat insert (gcctat) at position 1530 in exon 9 of KIT. CONCLUSION: Optimal management of gastrointestinal stromal tumor-induced hypoglycemia requires a multidisciplinary approach, and surgical debulking is the treatment of choice to obtain immediate symptom relief. Imatinib or combinations of glucocorticoids and growth hormone are alternative palliative strategies for symptomatic hypoglycemia. In addition, mutations in exon 9 of the tyrosine kinase receptor KIT occur in 11–20% of GIST and are often associated with poor patient outcomes. The association of this KIT mutation with non-islet cell tumor induced hypoglycemia has yet to be established
Treatment and outcomes of an Australian cohort of outpatients with bipolar 1 or schizoaffective disorder over twenty-four months : implications for clinical practice
- Author
- A Cipriani
- A Jablensky
- A Zutshi
- AJ Rush
- Alan JM Brnabic
- Amanda J Lowry
- American Psychiatric Association
- Anthony de Castella
- CJ Murray
- Collaborative Working Group on Clinical Trial Evaluations
- DJ Abrams
- DM Hilty
- DV Sheehan
- F Biffin
- GS Malhi
- GS Malhi
- GS Malhi
- GS Malhi
- GS Sachs
- I Goetz
- I Schillevoort
- J Kulkarni
- J Simon
- Jayashri Kulkarni
- JC Gomez
- JE Ware Jr
- JN Kogan
- K Benson
- Katarina Kelin
- Kate Filia
- KR Merikangas
- Lesley Berk
- LJ Williams
- LL Judd
- LN Yatham
- M Berk
- M Berk
- M Berk
- M Hamilton
- M Tohen
- M Tohen
- MB Keller
- Michael Berk
- MK Spearing
- MP Freeman
- MS Bauer
- National Institute for Health and Clinical Excellence
- Paul B Fitzgerald
- PF Buckley
- PR Rosenbaum
- R Baldessarini
- RB D'Agostino Jr
- RC Young
- RD Goldney
- RJ Baldessarini
- RW Lam
- S Dodd
- Sacha Filia
- Seetal Dodd
- The EuroQol Group
- William Montgomery
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2012
- Field of study
Background The Bipolar Comprehensive Outcomes Study (BCOS) is a 2-year, prospective, non-interventional, observational study designed to explore the clinical and functional outcomes associated with ‘real-world’ treatment of participants with bipolar I or schizoaffective disorder. All participants received treatment as usual. There was no study medication.Methods Participants prescribed either conventional mood stabilizers (CMS; n = 155) alone, or olanzapine with, or without, CMS (olanzapine ± CMS; n = 84) were assessed every 3 months using several measures, including the Young Mania Rating Scale, 21-item Hamilton Depression Rating Scale, Clinical Global Impressions Scale – Bipolar Version, and the EuroQol Instrument. This paper reports 24-month longitudinal clinical, pharmacological, functional, and socioeconomic data.Results On average, participants were 42 (range 18 to 79) years of age, 58%; were female, and 73%; had a diagnosis of bipolar I. Polypharmacy was the usual approach to pharmacological treatment; participants took a median of 5 different psychotropic medications over the course of the study, and spent a median proportion of time of 100%; of the study on mood stabilizers, 90%; on antipsychotics, 9%; on antidepressants, and 5%; on benzodiazepines/hypnotics. By 24 months, the majority of participants had achieved both symptomatic and syndromal remission of both mania and depression. Symptomatic relapse rates were similar for both the CMS alone (65%;) and the olanzapine ± CMS (61%;) cohorts.Conclusions Participants with bipolar I or schizoaffective disorder in this study were receiving complex medication treatments that were often discordant with recommendations made in contemporary major treatment guidelines. The majority of study participants demonstrated some clinical and functional improvements, but not all achieved remission of symptoms or syndrome.<br /
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
- Author
- Abecasis GR
- Abecasis GR
- Abecasis Goncalo R.
- Absher D
- Absher D
- Aherrahrou Z
- Ahmadi KR
- Alavere Helene
- Alizadeh Behrooz Z.
- Altshuler D
- Altshuler David
- Amin Najaf
- Andersen K
- Andrews JS
- Aragam J
- Arking DE
- Arnett DK
- Arora Pankaj
- Aspelund T
- Aspelund T
- Aspelund Thor
- Assime TL
- Assimes TL
- Assimes TL
- Atkinson EJ
- Attwood T
- Aulchenko YS
- Aulchenko YS
- Aulchenko YS
- Aulchenko Yurii
- Badola S
- Bakker SJ
- Ball SG
- Balmforth AJ
- Bandinelli Stefania
- Barbalic M
- Barroso In S.
- Beckmann J
- Beckmann Jacques S.
- Beilby John P.
- Bekaert S
- Belz S
- Benjamin E
- Benjamin EJ
- Benjamin EJ
- Bergman Richard N.
- Bergmann Sven
- Bickel C
- Bilo HJ
- Bis J
- Bis JC
- Bis JC
- Bis Joshua C
- Blankenberg S
- Blankenberg S
- Blankenberg S
- Blettner M
- Boban M
- Boban Mladen
- Bochud M
- Bochud Murielle
- Boehnke Michael
- Boerwinkle E
- Boerwinkle E
- Boerwinkle E
- Boerwinkle E
- Boerwinkle Eric
- Boomsma Dorret I.
- Borecki I
- Bragg-Gresham Jennifer L.
- Brandstätter A
- Braund P
- Braund PS
- Breteler Monique
- Brown MJ
- Bruse P
- Buckley Brendan
- Burke Gregory L
- Burnett MS
- Burtt N
- Böger CA
- Böhm BO
- Cambien F
- Cambien F
- Campbell H
- Campbell S
- Campbell Harry
- Caulfield MJ
- Caulfield Mark J.
- Cavalieri M
- Chakravarti Aravinda
- Chambers JC
- Chambers John C.
- Chang PP
- Chasman DI
- Chasman Daniel I.
- Chen IY
- Chen L
- Chen L
- Chen Yii-Der Ida
- Clarke Robert
- Cockcroft JR
- Collins Francis S.
- Connell JM
- Cook HT
- Cooper J
- Coresh J
- Cornelia M. McEniery CM
- Cornelis MC
- Corre Tanguy
- Corsi Anna Maria
- Cotlarciuc I
- Couper D
- Crisp-Hihn A
- Cupples L
- Cupples LA
- Cupples LA
- Curhan GC
- D'Adamo Adamo Pio
- Dandona S
- Davey Smith G
- Davies Gail
- de Andrade M
- De Backer GG
- De Bacquer D
- de Boer IH
- De Buyzere ML
- De Geus Eco J. C.
- de Jong PE
- De Meyer T
- de Silva R
- Deary Ian J.
- Debette Stéphanie
- Deckers JW
- Dehghan A
- Dehghan A
- Dehghan A
- Dehghan A
- Dehghan A
- Del Greco M Fabiola
- Deloukas P
- Deloukas P
- Demissie S
- Demissie-Banjaw S
- Deng G
- Destefano Anita L.
- Devaney J
- Devuyst O
- Dikkeschei LD
- Dimkovic N
- Ding J
- Dobnig H
- Dockrell M
- Doering A
- Dominiczak A
- Döring Angela
- Dörr M
- Dörr Marcus
- Eardman J
- Ebrahim S
- Eggermann T
- Ehret Georg B.
- Eiriksdottir G
- Eiriksdottir G
- Ellinghaus D
- Elliott P
- Elliott Paul
- Elosua R
- Emilsson Valur
- Endlich K
- Epstein SE
- Erdmann J
- Erdmann J
- Erdmann J
- Erdmann J
- Erdmann J
- Erdmann J
- Erdmann Jeanette
- Esko Tõnu
- Eyheramendy Susana
- Fabretto Antonella
- Facheris Maurizio
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- Farrall M
- Farrall Martin
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- Felix JF
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- Floege J
- Foad N
- Folsom A
- Folsom AR
- Fornage Myriam
- Forouhi NG
- Fortmann S
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- Fuchsberger C
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- Galan Pilar
- Gale DP
- Ganesh Santhi K.
- Gansevoort RT
- Gao X
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- Gider Pierre
- Gieger Christian
- Gillebert TC
- Glazer N
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- Glazer Nicole L.
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- Goodall AH
- Gottdiener JS
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- Gracey J
- Grammer TB
- Gray E
- Greiser KH
- Gretarsdottir S
- Groop Leif
- Grosshennig A
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- Gudnason V
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- Gyllensten Ulf B.
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- Hayward C
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- Krishnan U
- Kroemer HK
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- Kullo I
- Kundu Suman
- Kähönen Mika
- König IR
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- Köttgen A
- Kühnel Brigitte
- Laaksonen R
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- Laan Maris
- Lackner K
- Lackner KJ
- Lagou V
- Laitinen Jaana
- Lakatta EG
- Lapsley M
- Larson MG
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- Lathrop Mark
- Launer LJ
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- Launer Lenore
- Lawlor DA
- Leak TS
- Lehtimäki Terho
- Levy D
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- Lieb W
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- Linsel-Nitschke P
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- Liu Y
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- Lloyd-Jones H
- Loehr LR
- Lohman K
- Loitfelder Marisa
- Loley C
- Loos RJ
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- Lu Xiaowen
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- Lugauer I
- Lumley T
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- O'Reilly Paul F.
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- Olden M
- Ongen Halit
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- Reilly MP
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- Rice Kenneth M.
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- Rotter JI
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- Rudan I
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- Ruokonen A
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- Sala Cinzia
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- Ulivi Sheila
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- Van Duijn
- van Duijn C
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- Wareham NJ
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- Wichmann HE
- Wichmann HE
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- Witteman JC
- Witteman JC
- Witteman Jacqueline C. M.
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- Wright Alan F.
- Yang Q
- Yang YA
- Yasmin
- Zaboli G
- Zeginigg Marion
- Zeller T
- Zeller T
- Zeller T
- Zemunik T
- Zerres K
- Zgaga L
- Zhang W
- Zhang Feng
- Zhang Weihua
- Zhao Jing Hua
- Ziegler A
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- Ziegler A
- Zillikens MC
- Zitting Paavo
- Zweiker R
- Publication venue
- Nat Genet
- Publication date
- 01/01/2011
- Field of study
Numerous genetic loci have been associated with systolic blood pressure (SBP) and diastolic blood pressure (DBP) in Europeans. We now report genome-wide association studies of pulse pressure (PP) and mean arterial pressure (MAP). In discovery (N = 74,064) and follow-up studies (N = 48,607), we identified at genome-wide significance (P = 2.7 × 10(-8) to P = 2.3 × 10(-13)) four new PP loci (at 4q12 near CHIC2, 7q22.3 near PIK3CG, 8q24.12 in NOV and 11q24.3 near ADAMTS8), two new MAP loci (3p21.31 in MAP4 and 10q25.3 near ADRB1) and one locus associated with both of these traits (2q24.3 near FIGN) that has also recently been associated with SBP in east Asians. For three of the new PP loci, the estimated effect for SBP was opposite of that for DBP, in contrast to the majority of common SBP- and DBP-associated variants, which show concordant effects on both traits. These findings suggest new genetic pathways underlying blood pressure variation, some of which may differentially influence SBP and DBP
Theory and research in strategic management: Swings of a pendulum
- Author
- Alchian A. A.
- Almeida P.
- Amit R.
- Andrews K.
- Ansoff H. I.
- Bain J. S.
- Bain J. S.
- Barnard C. I.
- Barnett W. P.
- Barnett W. P.
- Barney J. B.
- Barney J. B.
- Barney J. B.
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The development of the field of strategic management within the last two decades has been dramatic. While its roots have been in a more applied area, often referred to as business policy, the current field of strategic management is strongly theory based, with substantial empirical research, and is eclectic in nature. This review of the development of the field and its current position examines the field’s early development and the primary theoretical and methodological bases through its history. Early developments include Chandler’s (1962) Strategy and Structure and Ansoff’s (1965) Corporate Strategy. These early works took on a contingency perspective (fit between strategy and structure) and a resource-based framework emphasizing internal strengths and weaknesses. Perhaps, one of the more significant contributions to the development of strategic management came from industrial organization (IO) economics, specifically the work of Michael Porter. The structure-conduct-performance framework and the notion of strategic groups, as well as providing a foundation for research on competitive dynamics, are flourishing currently. The IO paradigm also brought econometric tools to the research on strategic management. Building on the IO economics framework, the organizational economics perspective contributed transaction costs economics and agency theory to strategic management. More recent theoretical contributions focus on the resource-based view of the firm. While it has its roots in Edith Penrose’s work in the late 1950s, the resource-based view was largely introduced to the field of strategic management in the 1980s and became a dominant framework in the 1990s. Based on the resource-based view or developing concurrently were research on strategic leadership, strategic decision theory (process research) and knowledge-based view of the firm. The research methodologies are becoming increasingly sophisticated and now frequently combine both quantitative and qualitative approaches and unique and new statistical tools. Finally, this review examines the future directions, both in terms of theory and methodologies, as the study of strategic management evolves.Yeshttps://us.sagepub.com/en-us/nam/manuscript-submission-guideline
Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia
- Author
- Adams Mark
- Affonseca Bressan Rodrigo
- Agartz Ingrid
- Agerbo Esben
- Al Eissa Mariam
- Albus Margot
- Alexander Madeline
- Alizadeh Behrooz Z.
- Alptekin Köksal
- Als Thomas D.
- Amin Farooq
- Arolt Volker
- Arrojo Manuel
- Athanasiu Lavinia
- Atkinson Elizabeth G.
- Ausrele Kučinskiene Zita
- Awasthi Swapnil
- Azevedo Maria Helena
- Bacanu Silviu A.
- Bass Nicholas J.
- Begemann Martin
- Belliveau Richard A.
- Bene Judit
- Benyamin Beben
- Bergen Sarah E.
- Bigdeli Tim B.
- Blasi Giuseppe
- Bobes Julio
- Bonassi Stefano
- Braun Alice
- Bromet Evelyn J.
- Bruggeman Richard
- Bryois Julien
- Buckley Peter F.
- Buckner Randy L.
- Bybjerg-Grauholm Jonas
- Cahn Wiepke
- Cairns Murray J.
- Calkins Monica E.
- Carr Vaughan J.
- Castle David
- Catts Stanley V.
- Chambert Kimberley D.
- Chan Raymond C. K.
- Chaumette Boris
- Chen Chia-Yen
- Cheng Wei
- Cheung Eric F. C.
- Chong Siow Ann
- Cohen David
- Consoli Angele
- Cordeiro Quirino
- Costas Javier
- Curtis Charles
- Davidson Michael
- Davis Kenneth L.
- De Haan Lieuwe
- Degenhardt Franziska
- DeLisi Lynn E.
- Demontis Ditte
- Dennison Charlotte A.
- Dickerson Faith
- Dikeos Dimitris
- Dinan Timothy
- Djurovic Srdjan
- Duan Jubao
- Ducci Giuseppe
- Dudbridge Frank
- Eriksson Johan G.
- Fananas Lourdes
- Faraone Stephen V.
- Fiorentino Alessia
- Forstner Andreas
- Frank Josef
- Frei Oleksandr
- Freimer Nelson B.
- Fromer Menachem
- Frustaci Alessandra
- Gadelha Ary
- Ge Tian
- Genovese Giulio
- Gershon Elliot S.
- Giannitelli Marianna
- Giegling Ina
- Giusti-Rodríguez Paola
- Godard Stephanie
- Goldstein Jacqueline I.
- González Peñas Javier
- González-Pinto Ana
- Gopa Srihari
- Gratten Jacob
- Green Michael F.
- Greenwood Tiffany A.
- Grove Jakob
- Guillin Olivier
- Gur Raquel E.
- Gur Ruben C.
- Gutiérrez Blanca
- Gülöksüz Sinan
- Hahn Eric
- Hakonarson Hakon
- Hall Lynsey
- Haroutunian Vahram
- Hartmann Annette M.
- Harvey Carol
- Harwood Janet C.
- Hayward Caroline
- Henskens Frans A.
- Herms Stefan
- Hoffmann Per
- Howrigan Daniel P.
- Ikeda Masashi
- Iyegbe Conrad
- Joa Inge
- Julià Antonio
- Kam-Thong Tony
- Kamatani Yoichiro
- Karachanak-Yankova Sena
- Kebir Oussama
- Keller Matthew C.
- Kelly Brian J.
- Khrunin Andrey
- Kim Minsoo
- Kim Sung-Wan
- Klovins Janis
- Kondratiev Nikolay
- Konte Bettina
- Koopmans Frank
- Kraft Julia
- Kubo Michiaki
- Kusumawardhani Agung
- Kuzelov a-Ptackova Hana
- Kučinskas Vaidutis
- Kähler Anna K.
- Lam Max
- Land Stefano
- Lazzeroni Laura C.
- Lee Phil H.
- Legge Sophie E.
- Lehrer Douglas S.
- Lencer Rebecca
- Lerer Bernard
- Li Miaoxin
- Li Zhiqiang
- Lieberman Jeffrey
- Light Gregory A.
- Limborska Svetlana
- Liu Chih-Min
- Loughland Carmel M.
- Lubiski Jan
- Luykx Jurjen J.
- Lynham Amy
- Lönnqvist Jouko
- Macel Jr. Milan
- Mackinnon Andrew
- Magnusson Patrik K. E.
- Magnusson Sigurdur
- Maher Brion S.
- Maier Wolfgang
- Malaspina Dolores
- Mallet Jacques
- Marder Stephen R.
- Marsal Sara
- Martin Alicia R.
- Martorell Lourdes
- Mattheisen Manuel
- McCarley Robert W.
- McDonald Colm
- McGrath John J.
- Medeiros Helena
- Meier Sandra
- Melegh Bela
- Melle Ingrid
- Mesholam-Gately Raquelle I.
- Metspalu Andres
- Michie Patricia T.
- Milani Lili
- Milanova Vihara
- Mitjans Marina
- Molden Espen
- Molina Esther
- Molto María Dolores
- Mondelli Valeria
- Moreno Carmen
- Morley Christopher P.
- Muntané Gerard
- Murphy Kieran C.
- Myin-Germeys Inez
- Nenadić Igor
- Nestadt Gerald
- Neuchterlein Keith H.
- Nikitina-Zake Liene
- Noto Cristiano
- O'Brien Niamh Louise
- O'Neill F. Anthony.
- Oh Sang-Yun
- Olincy Ann
- Ota Vanessa Kiyomi
- Panagiotaropoulou Georgia
- Pantelis Christos
- Papadimitrou George N.
- Pardinas Antonio
- Paredella Mara
- Paurio Tiina
- Pellegrino Renata
- Periyasamy Sathish
- Perkins Diana O.
- Pfuhlmann Bruno
- Pietilainen Olli
- Pimm Jonathan
- Porteous David
- Powell John
- Qi Ting
- Quattrone Diego
- Quested Digby
- Radant Allen D.
- Rampino Antonio
- Rapaport Mark H.
- Rautanen Anna
- Reichenberg Abraham
- Richards Alexander L.
- Roe Cheryl
- Roffman Joshua L.
- Roth Julian
- Rothermundt Matthias
- Rutten Bart P. F.
- Saker-Delye Safaa
- Salomaa Veiko
- Sanjuan Julio
- Santoro Marcos Leite
- Savitz Adam
- Schall Ulrich
- Scott Rodney J.
- Seidman Larry J.
- Sharp Sally Isabel
- Shi Jianxin
- Sidorenko Julia
- Sigurdsson Engilbert
- Sim Kang
- Skarabis Nora
- Slominsky Petr
- So Hon-Cheong
- Sobell Janet L.
- Soderman Erik
- Stain Helen J.
- Steen Nils Eiel
- Steixner-Kumar Agnes
- Stogmann Elisabeth
- Stone William S.
- Straub Richard E.
- Stregman Eric
- Streit Fabian
- Stroup T. Scott
- Subramaniam Mythily
- Sugar Catherine A.
- Suvisaari Jaana
- Svrakic Dragan M.
- Swerdlow Neal R.
- Szatkiewicz Jin P.
- Ta Thi Minh Tam
- Takahashi Atsushi
- Terao Chikashi
- Thibaut Florence
- Toncheva Draga
- Tooney Paul A.
- Torretta Silvia
- Tosato Sarah
- Trubetskoy Vassily
- Tura Gian Battista
- Turetsky Bruce I.
- Ucock Alp
- Vaaler Arne
- Van Amelsvoort Therese
- Van Winkel Ruud
- Veijola Juha
- Voloudakis Georgios
- Waddington John
- Walter Henrik
- Watanabe Kyoto
- Waterreus Anna
- Webb Bradley T.
- Weiser Mark
- Williams Nigel M.
- Witt Stephanie H.
- Wormley Brandon K.
- Wu Jing Qin
- Wu Yang
- Xu Zhida
- Yolken Robert
- Zai Clement C.
- Zeng Jian
- Zhang Wen
- Zhou Wei
- Zhu Feng
- Zimprich Fritz
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 21/04/2022
- Field of study
Schizophrenia has a heritability of 60–80%1, much of which is attributable to common risk alleles. Here, in a two-stage genome-wide association study of up to 76,755 individuals with schizophrenia and 243,649 control individuals, we report common variant associations at 287 distinct genomic loci. Associations were concentrated in genes that are expressed in excitatory and inhibitory neurons of the central nervous system, but not in other tissues or cell types. Using fine-mapping and functional genomic data, we identify 120 genes (106 protein-coding) that are likely to underpin associations at some of these loci, including 16 genes with credible causal non-synonymous or untranslated region variation. We also implicate fundamental processes related to neuronal function, including synaptic organization, differentiation and transmission. Fine-mapped candidates were enriched for genes associated with rare disruptive coding variants in people with schizophrenia, including the glutamate receptor subunit GRIN2A and transcription factor SP4, and were also enriched for genes implicated by such variants in neurodevelopmental disorders. We identify biological processes relevant to schizophrenia pathophysiology; show convergence of common and rare variant associations in schizophrenia and neurodevelopmental disorders; and provide a resource of prioritized genes and variants to advance mechanistic studies
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Observation of electroweak production of two jets in association with an isolated photon and missing transverse momentum, and search for a Higgs boson decaying into invisible particles at 13 TeV with the ATLAS detector
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- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abud A Abed
- Abulaiti Y
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Addepalli SV
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Agullo P Martinez
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ai X
- Aielli G
- Aizenberg I
- Akatsuka S
- Akbiyik M
- Akesson TPA
- Akimov AV
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
- Alhroob M
- Ali B
- Ali S
- Aliev M
- Alimonti G
- Allaire C
- Allbrooke BMM
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alves FL Lucio
- Alviggi MG
- Ambler A
- Ambroz L
- Amelung C
- Amidei D
- Amoroso S
- Amrouche CS
- Anastopoulos C
- Andana RY Gonzalez
- Andari N
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Angelidakis S
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antipov E
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- Zhou N
- Zhou Y
- Zhu C
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinsser J
- Ziolkowski M
- Zivkovic L
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Publication venue
- EUROPEAN PHYSICAL JOURNAL C
- Publication date
- 03/02/2022
- Field of study
This paper presents the measurement of the electroweak production of two jets
in association with a Zγ pair with the Z boson decaying into two
neutrinos. It also presents the search for invisible or partially invisible
decays of a Higgs boson with a mass of 125 GeV produced through vector-boson
fusion with a photon in the final state. These results use data from LHC
proton-proton collisions at s = 13 TeV collected with the ATLAS
detector corresponding to an integrated luminosity of 139 fb−1. The event
signature, shared by all benchmark processes considered for measurements and
searches, is characterized by a significant amount of unbalanced transverse
momentum and a photon in the final state, in addition to a pair of forward
jets. For electroweak production of Zγ in association with two jets, the
background-only hypothesis is rejected with an observed (expected) significance
of 5.2 (5.1) standard deviations. The measured fiducial cross-section for this
process is 1.31±0.29 fb. Observed (expected) upper limit of 0.37 (0.34) at
95% confidence level is set on the branching ratio of a 125 GeV Higgs boson to
invisible particles, assuming the Standard Model production cross-section. The
signature is also interpreted in the context of decays of a Higgs boson to a
photon and a dark photon. An observed (expected) 95% CL upper limit on the
branching ratio for this decay is set at 0.018 (0.017), assuming the 125 GeV
Standard Model Higgs boson production cross-section
Recommended from our members
The ATLAS inner detector trigger performance in pp collisions at 13 TeV during LHC Run 2
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abud A Abed
- Abulaiti Y
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Agullo P Martinez
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ahnen J Von
- Ai X
- Aielli G
- Akatsuka S
- Akbiyik M
- Akesson TPA
- Akilli E
- Akimov AV
- Alberghi GL
- Albert J
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- Aleksa M
- Aleksandrov IN
- Alexa C
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- Publication venue
- EUROPEAN PHYSICAL JOURNAL C
- Publication date
- 08/03/2022
- Field of study
The design and performance of the inner detector trigger for the high level
trigger of the ATLAS experiment at the Large Hadron Collider during the 2016-18
data taking period is discussed. In 2016, 2017, and 2018 the ATLAS detector
recorded 35.6 fb−1, 46.9 fb−1, and 60.6 fb−1 respectively of
proton-proton collision data at a centre-of-mass energy of 13 TeV. In order to
deal with the very high interaction multiplicities per bunch crossing expected
with the 13 TeV collisions the inner detector trigger was redesigned during the
long shutdown of the Large Hadron Collider from 2013 until 2015. An overview of
these developments is provided and the performance of the tracking in the
trigger for the muon, electron, tau and b-jet signatures is discussed. The
high performance of the inner detector trigger with these extreme interaction
multiplicities demonstrates how the inner detector tracking continues to lie at
the heart of the trigger performance and is essential in enabling the ATLAS
physics programme
The ATLAS inner detector trigger performance in pp collisions at 13 TeV during LHC Run 2
- Author
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- Publication venue
- EUROPEAN PHYSICAL JOURNAL C
- Publication date
- 01/01/2022
- Field of study
The design and performance of the inner detector trigger for the high level
trigger of the ATLAS experiment at the Large Hadron Collider during the 2016-18
data taking period is discussed. In 2016, 2017, and 2018 the ATLAS detector
recorded 35.6 fb−1, 46.9 fb−1, and 60.6 fb−1 respectively of
proton-proton collision data at a centre-of-mass energy of 13 TeV. In order to
deal with the very high interaction multiplicities per bunch crossing expected
with the 13 TeV collisions the inner detector trigger was redesigned during the
long shutdown of the Large Hadron Collider from 2013 until 2015. An overview of
these developments is provided and the performance of the tracking in the
trigger for the muon, electron, tau and b-jet signatures is discussed. The
high performance of the inner detector trigger with these extreme interaction
multiplicities demonstrates how the inner detector tracking continues to lie at
the heart of the trigger performance and is essential in enabling the ATLAS
physics programme
Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease
- Author
- Aaltonen M
- Abdur Rahman M
- Abell T
- Abide W. Jr
- Acheatel R
- Achiri P
- Acon J
- Adams T
- Affinito S
- Agarwal S
- Aggarwal K
- Aggarwal R
- Ahlström P
- Ahmad A
- Ahmed M
- Aillon C
- Airaksinen A
- Ait-sadi R
- Akers J
- Al-jumaily J
- Albers C
- Albert M
- Alberti A
- Alexander T
- Alford C
- Algotsson L
- Allen T
- Allworth M
- Almond E
- Aloisi A
- Alternburg C
- Alton M
- Amin J
- Amundson A
- Andersen K
- Andersen M
- Anderson E
- Anderson G
- Anderson R
- Anderson T
- Andersson H
- Andersson L
- Andreo J
- Andres C
- Andresen D
- Andrews G
- Andrews L
- Andrews R
- Andrioli V
- Angermann Ce
- Annas T
- Ansell V
- Antonio-drabek C
- Antonishen D
- Antonishen M
- Anuschek V
- Appel Kf
- Appel S
- Appleyard D
- Archer A
- Armitage J
- Armstrong L
- Armstrong M
- Arnesson K
- Arnold M
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- Arp H
- Asbill B
- Ashbrook-raby C
- Ashton L
- Assarsson E
- Audet K
- Augenbraun C
- Aung HNIN THANDA
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- Ausner J
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- Awasty V
- Axelsson U
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- Ayub H
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- Babington G
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- Baghiana S
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- Bai J
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- Bansilal S
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- Zhao L
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- Zhou Xingyu
- Zhou Yingyuan
- Zhu Wangqin
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- Zuchelkowski A
- Zulauf N
- Ågårdh A
- Öner A
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND:
Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes.
METHODS:
We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization.
RESULTS:
During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events.
CONCLUSIONS:
Among patients with atherosclerotic vascular disease who were receiving intensive statin therapy, the use of anacetrapib resulted in a lower incidence of major coronary events than the use of placebo. (Funded by Merck and others; Current Controlled Trials number, ISRCTN48678192 ; ClinicalTrials.gov number, NCT01252953 ; and EudraCT number, 2010-023467-18 .)
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